Canonical Allele Identifier: CA913180181
Gene:

Linked Data

ClinVar Variation Id: 689972
ClinVar RCV Id: RCV000850829
dbSNP Id: rs1603220083

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5669G>A , J01415.2:m.5669G>A GRCh38